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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894584Generated: October 28, 2026

2,6-Dimethylaniline → HCID 20512402, compound

https://huagongshe.com/reaction/894584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethylanilineHCID 6896—
ReactantHCID 20512395HCID 20512395—
CatalystPotassium IodideHCID 4875—
SolventHydrochloric AcidHCID 313—
ProductHCID 20512402HCID 2051240275.3%

Reaction Steps

A mixture of 106.8 g (0.441 moles) of N-(β-bromopropyl)-2,6-dimethyl-aniline, obtained as described in point (a) above, 110 ml (107.4 g, 0.88 moles) of 2,6-dimethylaniline and 1.6 g (10 mmoles) of potassium iodide is stirred at 100° to 105° C. for 3 hours under nitrogen atmosphere. The mixture is allowed to cool, 600 ml of 10% aqueous hydrochloric acid are added, and the resulting mixture is allowed to stand at room temperature overnight. The separated precipitate, which is a mixture of the hydrochloride and the hydrobromide of the expected product, is filtered off, washed with water, dried, and then treated as described in point (b) of Method (b) above in order to liberate the base. In this way 93.8 g (75.3%) of 1,2-bis(2',6'-dimethylphenyl-amino)-propane are obtained; m.p.: 54°-56° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284642
Source datasetuspto-grants-1981_08
ORD IDord-9ba83dfb20d0468fb146f6c62cb68d12
Source noteuspto-grants-1981_08